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Beckman Coulter, Inc.
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SYNCHRON CX PRO CLINICAL SYSTEMS, MODEL CX4 PRO, CX5 PRO, CX7 PRO, CX9 PRO is an FDA 510(k)-cleared medical device (K011465) manufactured by Beckman Coulter, Inc.. This device is classified under the Clinical Toxicology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 7, 2001. Regulation: 8.